Canonical Allele Identifier: CA270114402

Gene: B2M

Linked Data

• dbSNP Id: rs11553044
• gnomAD v4: 15-44711582-A-G
• MyVariant Identifiers: chr15:g.45003780A>G (hg19) ; chr15:g.44711582A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711582A>G , CM000677.2:g.44711582A>G	GRCh38
NC_000015.9:g.45003780A>G , CM000677.1:g.45003780A>G	GRCh37
NC_000015.8:g.42791072A>G	NCBI36
NG_012920.1:g.5096A>G
NG_012920.2:g.5106A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695792.1:n.83+142A>G
ENST00000648006.3:c.36A>G MANE Select	ENSP00000497910.1:p.Leu12=
ENST00000349264.10:c.36A>G	ENSP00000340858.6:p.Leu12=
ENST00000544417.5:c.36A>G	ENSP00000437604.2:p.Leu12=
ENST00000557901.5:c.36A>G	ENSP00000452861.1:p.Leu12=
ENST00000558401.5:c.36A>G	ENSP00000452780.1:p.Leu12=
ENST00000559720.5:n.96A>G
ENST00000559916.1:c.36A>G	ENSP00000453350.1:p.Leu12=
ENST00000561424.5:c.36A>G	ENSP00000453191.1:p.Leu12=
NM_004048.2:c.36A>G	NP_004039.1:p.Leu12=
XM_005254549.2:c.36A>G	XP_005254606.1:p.Leu12=
NM_004048.3:c.36A>G	NP_004039.1:p.Leu12=
XM_005254549.3:c.36A>G	XP_005254606.1:p.Leu12=
XR_002957658.1:n.91A>G
NM_004048.4:c.36A>G MANE Select	NP_004039.1:p.Leu12=